NDC 68915-256 Avva Vaginal

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
68915-256
Proprietary Name:
Avva Vaginal
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Eastern Century Pharmaceuticals
Labeler Code:
68915
Start Marketing Date: [9]
05-20-2011
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 68915-256-02

Package Description: 1 BOTTLE in 1 BOX / 5.5 mL in 1 BOTTLE (68915-256-01)

Product Details

What is NDC 68915-256?

The NDC code 68915-256 is assigned by the FDA to the product Avva Vaginal which is product labeled by Eastern Century Pharmaceuticals. The product's dosage form is . The product is distributed in a single package with assigned NDC code 68915-256-02 1 bottle in 1 box / 5.5 ml in 1 bottle (68915-256-01). This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Avva Vaginal?

Stop use and ask doctor if: Rash or irritation and redness develops.Discontinue use if any burning, itching, or irritation of the vagina occurs during use. Wash and douche with water.  Do not douche to prevent pregnancy During pregnancyIf you have symptoms of pelvic inflammatory disease (PID) or sexually transmitted disease (STD) To self treat or prevent a STD or PIDAfter exposure to STD stop using this product and consult a doctor if douching results in pain, soreness, swelling, redness, itching excessive dryness or irritation, or symptoms continue after 7 days. These may indicate a serious condition.

Which are Avva Vaginal UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Avva Vaginal Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Avva Vaginal?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".